Overview

Evaluation of Gastrointestinal Transit Pre and Pos Treatment With Non Selective Betablocker in a Population of Cirrhotics

Status:
Unknown status
Trial end date:
2021-05-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to evaluate the influence of non betablockers in gastrointestinal motility (transit time) in patients with liver cirrhosis.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
ALDO TORRE DELGADILLO
Treatments:
Adrenergic beta-Antagonists
Propranolol
Criteria
Inclusion Criteria:

- Cirrhosis of any ethiology

- Child Pugh A, B, C without beta-blocker treatment previously (min. 1 month without
treatment)

- Patients with previous variceal bleeding (with liver cirrhosis) * Patients with
ascites or bacterial spontaneous peritonitis

Exclusion Criteria:

- Variceal disease without cirrhosis

- Cirrhotics patients that use antibiotics, prebiotics and probiotics during the study
period and one month previously

- Patients under immunosuppressor treatment

- Patients with portal thrombosis

- Patients with Sd. Budd-Chiari or cava/suprahepatic thrombosis

- Patients with active infection process